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Disseminated De Novo Myeloid Sarcoma in a 17-year-old Boy
Disseminated De Novo Myeloid Sarcoma in a 17-year-old Boy
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Disseminated De Novo Myeloid Sarcoma in a 17-year-old Boy

Sandre, Matthew K ; Liu, Annie ; Levy, Rebecca

Pediatric dermatology, 2019, Vol.36 (4), p.509-510

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2
A case of recalcitrant silicone granuloma treated with adalimumab: A case report
A case of recalcitrant silicone granuloma treated with adalimumab: A case report
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A case of recalcitrant silicone granuloma treated with adalimumab: A case report

Silverberg, Orli M ; Cyrenne, Benoit M ; Croitoru, David ; Sandre, Matthew K ; Pon, Kucy

SAGE open medical case reports, 2022, Vol.10, p.2050313X221093444-2050313X221093444

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3
Is It Only Takotsubo Syndrome? Cardiac MRI and a Case of Delayed ST-Elevation
Is It Only Takotsubo Syndrome? Cardiac MRI and a Case of Delayed ST-Elevation
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Is It Only Takotsubo Syndrome? Cardiac MRI and a Case of Delayed ST-Elevation

Sandre, Anthony R ; Leong, Darryl P ; Landry, David ; Martin, Leslie J

CJC open, 2020, Vol.2 (6), p.722-725

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4
GRS Nubes Supra Lunam, a New Lunula Shape
GRS Nubes Supra Lunam, a New Lunula Shape
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GRS Nubes Supra Lunam, a New Lunula Shape

Sandre, Matthew K ; Rohekar, Sherry ; Guenther, Lyn

Journal of cutaneous medicine and surgery, 2015, Vol.19 (6), p.528-529

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5
Lamin A/C gene (LMNA) mutation associated with laminopathy: A rare cause of idiopathic acro-osteolysis
Lamin A/C gene (LMNA) mutation associated with laminopathy: A rare cause of idiopathic acro-osteolysis
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Lamin A/C gene (LMNA) mutation associated with laminopathy: A rare cause of idiopathic acro-osteolysis

Lambert, Julie-Charlotte ; Baudart, Pauline ; De Sandre-Giovannoli, Annachiara ; Molin, Arnaud ; Marcelli, Christian

Joint bone spine, 2019, Vol.86 (4), p.525-527

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6
An elderly long-term care resident with crusted scabies
An elderly long-term care resident with crusted scabies
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An elderly long-term care resident with crusted scabies

Sandre, Matthew ; Ralevski, Filip ; Rau, Neil

The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale, 2015, Vol.26 (1), p.39-40

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7
Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype
Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype
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Case Report: Identification of Novel Variants in ERCC4 and DDB2 Genes in Two Tunisian Patients With Atypical Xeroderma Pigmentosum Phenotype

Nabouli, Imen ; Chikhaoui, Asma ; Othman, Houcemeddine ; Elouej, Sahar ; Jones, Meriem ; Lagarde, Arnaud ; Rekaya, Meriem Ben ; Messaoud, Olfa ; Zghal, Mohamed ; Delague, Valerie ; Levy, Nicolas ; De Sandre-Giovannoli, Annachiara ; Abdelhak, Sonia ; Yacoub-Youssef, Houda

Frontiers in genetics, 2021, Vol.12, p.650639-650639

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8
A novel overlapping phenotype characterized by lipodystrophy, mandibular dysplasia, and dilated cardiomyopathy associated with a new mutation in the LMNA gene
A novel overlapping phenotype characterized by lipodystrophy, mandibular dysplasia, and dilated cardiomyopathy associated with a new mutation in the LMNA gene
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A novel overlapping phenotype characterized by lipodystrophy, mandibular dysplasia, and dilated cardiomyopathy associated with a new mutation in the LMNA gene

Ambrosi, Pierre ; Kreitmann, Bernard ; Lepidi, Hubert ; Habib, Gilbert ; Levy, Nicolas ; Philip, Nicole ; De Sandre-Giovannoli, Annachiara

International journal of cardiology, 2016, Vol.209, p.317-318

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9
Toward Ultrasonic Tunable Ultra-Damping Metamaterials
Toward Ultrasonic Tunable Ultra-Damping Metamaterials
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Toward Ultrasonic Tunable Ultra-Damping Metamaterials

Mondain-Monval, Oliver ; Sandre, O ; Brunet, T ; Poncelet, O ; Aristegui, C ; Leng, J ; Mascaro, B ; Zimny, K ; Aradian, A

2014

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10
A collodion baby with facial dysmorphism, limb anomalies, pachygyria and genital hypoplasia: a mild form of Neu-laxova syndrome or a new entity?
A collodion baby with facial dysmorphism, limb anomalies, pachygyria and genital hypoplasia: a mild form of Neu-laxova syndrome or a new entity?
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A collodion baby with facial dysmorphism, limb anomalies, pachygyria and genital hypoplasia: a mild form of Neu-laxova syndrome or a new entity?

Ozcan, Deren ; Derbent, Murat ; Seçkin, Deniz ; Bikmaz, Yunus Emre ; Ağildere, Muhteşem ; De Sandre-Giovannoli, Annachiara ; Lévy, Nicolas ; Gürakan, Berkan

Annals of dermatology, 2013, Vol.25 (4), p.483-488

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